Partnering Solutions

  1. Full-Service Clinical Development Solutions 9/27/2023

    Getting a novel therapy through the clinical development process to approval is complicated. Unearth how to advance novel medical therapies from Phase I-III clinical development to market with confidence.

  2. Support For Institutions 4/5/2022

    At Advarra, our mission is to advance clinical research: safer, smarter, faster. This mission is embodied in everything we do, starting with our experienced staff, many of whom come from esteemed institutions and organizations within the clinical research community.

  3. Transforming Clinical Trial Site Forecasting 10/30/2024

    In today’s ever-evolving clinical trial space, managing the expenses associated with conducting a study is more important – and fraught – than ever before.

  4. pci | bridge: Real-Time Supply Chain Information 6/1/2023

    Unlock an enhanced customer experience through digital transformation by applying real-time visibility into your supply chain using cross-functional workflows and data-driven insights.

  5. Introducing One Home for Sites™ 2/8/2024

    One Home for Sites is a vendor-agnostic, sponsor-agnostic, aggregation platform that provides single sign-on and more. Become part of the only industry-wide solution to site tech overload.

  6. How Biorasi Optimizes Clinical Solutions 4/26/2019

    Best-in-class processes coupled with industry-leading technology to fight for your trial’s success.

  7. Novotech Drug Development Consulting: Services For Success 6/27/2023

    Delve into the details of this full-service global product development and strategic regulatory group that has a proven track record of successful FDA meetings and approvals.

  8. Integrated Services And Trusted Scientific Insight 3/17/2025

    Uncover how we're able to bring integrated services and trusted scientific insight to every molecule and program.

  9. RegOps Services To Streamline Regulatory Submissions 5/28/2024

    Our RegOps team offers document-level publishing or management of the entire regulatory submission process. Coupled with our electronic document management system (Veeva), we can oversee all technical aspects for submission of your dossier (eg, eCTD document granularity, utilization of content templates, document formatting, hyperlinking, bookmarks, navigation, publishing, and redaction services).

  10. OneScout: Guiding Patients, Sites, Sponsors, And CROs Every Step Of The Way 12/6/2024

    From start-up to close-out, Scout helps trials stay on track, patients stick with it, and sites maximize their time and resources.